Li Y H, Gu G Z, Zhou W H, Wu H, Chen G S, Zhang H L, Zheng Y X, Yu S F
Henan Provincial Institute for Occupational Health, Zhengzhou 450052, China.
Wugang Institute for Occupational Health, Wugang 462599, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2020 Feb 20;38(2):120-124. doi: 10.3760/cma.j.issn.1001-9391.2020.02.009.
To investigate the association between the single nucleotide polymorphisms (SNPS) at rs1695 and rs6591256 in glutathione S-transferase P1 (GSTP1) gene and susceptibility to noise-induced hearing loss in Chinese Han workers exposed to noise. A 1: 2 matched nested case-control study was performed, which based on the cohort of 6297 workers exposed to noise in an iron and steel plant in Henan, China, who were followed up from January 1, 2006 to December 31, 2015. According to the criteria of binaural average high-frequency hearing threshold ≥40 dB, a total of 292 workers were enrolled as hearing loss group; after the adjustment for sex, type of work, age (difference≤5 years) , and working years of noise exposure (difference≤2 years) , according to the criteria of binaural average high-frequency hearing threshold <35 dB, and the speech frequency hearing threshold of any ear at any frequency band ≤25 dB, a total of 584 workers were enrolled as control group. The single nucleotide polymorphisms (SNPs) of rs1695 and rs6591256 in GSTP1 were genotyped by high throughput SNP genotyping assay. Hardy-Weinberg equilibrium of control group was checked. The association between the SNPs at the two loci and susceptibility to NIHL was analyzed. The L(Aeq, 8 h) range of workers exposed to noise was 80.2-98.8 dB (A) . The risk of NIHL in individuals with allele G of rs1695 was 1.291 times of those with allele A (95%: 1.042-1.598, <0.05) . The risk of NIHL in individuals with allele G of rs6591256 was 1.390 times of those with allele A (95%: 1.119-1.728, <0.05) . The risk of NIHL in individuals with AG and GG genotypes of rs6591256 was 1.437 times of those with AA genotype (95%: 1.057-1.952, <0.05) . With the increase of noise exposure duration, individuals with AG and GG genotypes of rs6591256 had a higher risk of NIHL than those with AA genotype (HR=1.273, 95%: 1.002-1.616, <0.05) . The allele G of rs1695 and rs6591256 may be risk factors of NIHL.
探讨谷胱甘肽S-转移酶P1(GSTP1)基因rs1695和rs6591256位点的单核苷酸多态性(SNPs)与中国汉族噪声暴露工人噪声性听力损失易感性之间的关联。进行了一项1:2匹配的巢式病例对照研究,该研究基于中国河南一家钢铁厂6297名噪声暴露工人的队列,这些工人于2006年1月1日至2015年12月31日接受随访。根据双耳平均高频听力阈值≥40dB的标准,共纳入292名工人作为听力损失组;在对性别、工作类型、年龄(差异≤5岁)和噪声暴露工龄(差异≤2年)进行调整后,根据双耳平均高频听力阈值<35dB以及任一耳在任何频段的言语频率听力阈值≤25dB的标准,共纳入584名工人作为对照组。采用高通量SNP基因分型检测法对GSTP1基因rs1695和rs6591256位点的单核苷酸多态性(SNPs)进行基因分型。检查对照组的Hardy-Weinberg平衡。分析两个位点的SNPs与噪声性听力损失易感性之间的关联。噪声暴露工人的等效连续A声级(L(Aeq, 8 h))范围为80.2 - 98.8dB(A)。rs1695位点携带G等位基因的个体发生噪声性听力损失的风险是携带A等位基因个体的1.291倍(95%可信区间:1.042 - 1.598,P<0.05)。rs6591256位点携带G等位基因的个体发生噪声性听力损失的风险是携带A等位基因个体的1.390倍(95%可信区间:1.119 - 1.728,P<0.05)。rs6591256位点AG和GG基因型个体发生噪声性听力损失的风险是AA基因型个体的1.437倍(95%可信区间:1.057 - 1.952,P<0.05)。随着噪声暴露时长增加,rs6591256位点AG和GG基因型个体发生噪声性听力损失的风险高于AA基因型个体(风险比=1.273,95%可信区间:1.002 - 1.616,P<0.05)。rs1695和rs6591256位点的G等位基因可能是噪声性听力损失的危险因素。